Recurrent bacterial skin infections

Symptom Information:

Symptom ID: HPO:0005406
Synonyms:
Recurrent cutaneous pyogenic infections [HPO:0005406]
Recurrent episodes of impetigo [HPO:0005406]
Recurrent episodes of infectious dermatitis [HPO:0005406]
Recurrent pyogenic skin infections [HPO:0005406]
Recurrent bacterial skin infections [OMIM:Recurrent bacterial skin infections]
Recurrent pyogenic skin infections [OMIM:Recurrent pyogenic skin infections]
Quality:
Cross references:
OMIM: "Recurrent bacterial skin infections" [OMIM:Recurrent bacterial skin infections]
OMIM: "Recurrent pyogenic skin infections" [OMIM:Recurrent pyogenic skin infections]
Is a (Direct Parents):
HPO         Recurrent bacterial infections
HPO         Recurrent skin infections
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent bacterial infections(HPO:0002718)
                   Recurrent bacterial skin infections(HPO:0005406)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin physiology(HPO:0011122)
                   Inflammatory abnormality of the skin(HPO:0011123)
                      Recurrent skin infections(HPO:0001581)
                         Recurrent bacterial skin infections(HPO:0005406)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE (OMIM:233690)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I (OMIM:233700)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE II (OMIM:233710)
GRANULOMATOUS DISEASE, CHRONIC, X-LINKED (OMIM:306400)
Haim-Munk syndrome (Orphanet:2342)
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT (OMIM:148210)
KID syndrome (Orphanet:477)